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C A Stolle

Showing results (21-30 of 30) with videos related to

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Matrix (Stuttgart, Germany)|August 1, 1991
Mammalian tropoelastin: multiple domains of the protein define an evolutionarily divergent amino acid sequenceC D Boyd, A M Christiano, R A Pierce, et al.
American Journal of Medical Genetics|February 6, 1999
TWIST gene mutation in a patient with radial aplasia and craniosynostosis: further evidence for heterogeneity of Baller-Gerold syndromeK W Gripp, C A Stolle, L Celle, et al.
Matrix (Stuttgart, Germany)|November 1, 1991
Alternative splicing of rat tropoelastin mRNA is tissue-specific and developmentally regulatedR A Heim, R A Pierce, S B Deak, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 15, 2000
Frataxin point mutations in two patients with Friedreich's ataxia and unusual clinical featuresM L McCormack, R P Guttmann, M Schumann, et al.
The Journal of Clinical Investigation|July 1, 1989
Expression of multiple Na+,K+-adenosine triphosphatase isoform genes in human hematopoietic cells. Behavior of the novel A3 isoform during induced maturation of HL60 cellsM Gilmore-Hebert, J W Schneider, A L Greene, et al.
Annals of the New York Academy of Sciences|November 18, 1996
Multiple defects in type III collagen synthesis are associated with the pathogenesis of abdominal aortic aneurysmsD W Anderson, T K Edwards, M H Ricketts, et al.
American Journal of Medical Genetics|August 26, 1998
Phenotype of the fibroblast growth factor receptor 2 Ser351Cys mutation: Pfeiffer syndrome type IIIK W Gripp, C A Stolle, D M McDonald-McGinn, et al.
Human Mutation|January 1, 1995
Aberrant splicing of the type III procollagen mRNA leads to intracellular degradation of the protein in a patient with Ehlers-Danlos type IVS Thakker-Varia, D W Anderson, H Kuivaniemi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 3, 2001
A diagnostic approach to identifying submicroscopic 7p21 deletions in Saethre-Chotzen syndrome: fluorescence in situ hybridization and dosage-sensitive Southern blot analysisK W Gripp, V Kasparcova, D M McDonald-McGinn, et al.
Human Molecular Genetics|August 15, 2000
Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactionsR H Crosbie, L E Lim, S A Moore, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Matrix (Stuttgart, Germany)|August 1, 1991
Mammalian tropoelastin: multiple domains of the protein define an evolutionarily divergent amino acid sequenceC D Boyd, A M Christiano, R A Pierce, et al.
American Journal of Medical Genetics|February 6, 1999
TWIST gene mutation in a patient with radial aplasia and craniosynostosis: further evidence for heterogeneity of Baller-Gerold syndromeK W Gripp, C A Stolle, L Celle, et al.
Matrix (Stuttgart, Germany)|November 1, 1991
Alternative splicing of rat tropoelastin mRNA is tissue-specific and developmentally regulatedR A Heim, R A Pierce, S B Deak, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 15, 2000
Frataxin point mutations in two patients with Friedreich's ataxia and unusual clinical featuresM L McCormack, R P Guttmann, M Schumann, et al.
The Journal of Clinical Investigation|July 1, 1989
Expression of multiple Na+,K+-adenosine triphosphatase isoform genes in human hematopoietic cells. Behavior of the novel A3 isoform during induced maturation of HL60 cellsM Gilmore-Hebert, J W Schneider, A L Greene, et al.
Annals of the New York Academy of Sciences|November 18, 1996
Multiple defects in type III collagen synthesis are associated with the pathogenesis of abdominal aortic aneurysmsD W Anderson, T K Edwards, M H Ricketts, et al.
American Journal of Medical Genetics|August 26, 1998
Phenotype of the fibroblast growth factor receptor 2 Ser351Cys mutation: Pfeiffer syndrome type IIIK W Gripp, C A Stolle, D M McDonald-McGinn, et al.
Human Mutation|January 1, 1995
Aberrant splicing of the type III procollagen mRNA leads to intracellular degradation of the protein in a patient with Ehlers-Danlos type IVS Thakker-Varia, D W Anderson, H Kuivaniemi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 3, 2001
A diagnostic approach to identifying submicroscopic 7p21 deletions in Saethre-Chotzen syndrome: fluorescence in situ hybridization and dosage-sensitive Southern blot analysisK W Gripp, V Kasparcova, D M McDonald-McGinn, et al.
Human Molecular Genetics|August 15, 2000
Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactionsR H Crosbie, L E Lim, S A Moore, et al.
Pageof 3